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Alkane Carbonylation with Carbon Monoxide on Sulfated Zirconia: NMR Observation of Ketone and Carboxylic Acid Formation from Isobutane and CO Full article

Journal Angewandte Chemie - International Edition
ISSN: 1433-7851 , E-ISSN: 1521-3773
Output data Year: 2000, Volume: 39, Number: 20, Pages: 3658-3660 Pages count : 3 DOI: 10.1002/1521-3773(20001016)39:20<3658::AID-ANIE3658>3.0.CO;2-C
Tags SOLID-STATE NMR ; H/D EXCHANGE; ISOMERIZATION; ACTIVATION; CATALYST; BUTANE
Authors Stepanov Alexander G. 1 , Luzgin Mikhail V. 1 , Krasnoslobodtsev Alexey V. 2 , Shmachkova Vera P. 1 , Kotsarenko Nina S. 1
Affiliations
1 Group of NMR Spectroscopy for Catalytic Hydrocarbon Conversion and Laboratory for Zeolites and Acid-Base Catalysis, Boreskov Institute of Catalysis Siberian Branch, Russian Academy of Sciences
2 Natural Science Department, Novosibirsk State University

Funding (2)

1 Russian Foundation for Basic Research 99-03-32454
2 International Association for the Promotion of Co-operation with Scientists from the New Independent States of the Former Soviet Union 95-0194

Abstract: Coadsorbed water determines the reaction products when isobutane undergoes carbonylation by CO on a sulfated zirconia catalyst at 70°C. This is shown by the results of in situ solid-state 13C NMR and ex situ 13C high-resolution NMR spectroscopy and by GC-MS analyses. Methyl isopropyl ketone selectively forms in the absence of water, while pivalic acid represents the primary reaction product the presence of coadsorbed water (see scheme).
Cite: Stepanov A. , Luzgin M. , Krasnoslobodtsev A. , Shmachkova V. , Kotsarenko N.
Alkane Carbonylation with Carbon Monoxide on Sulfated Zirconia: NMR Observation of Ketone and Carboxylic Acid Formation from Isobutane and CO
Angewandte Chemie - International Edition. 2000. V.39. N20. P.3658-3660. DOI: 10.1002/1521-3773(20001016)39:20<3658::AID-ANIE3658>3.0.CO;2-C WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Mar 17, 2000
Accepted: Jul 17, 2000
Published online: Oct 13, 2000
Published print: Oct 16, 2000
Identifiers:
Web of science: WOS:000090010000026
Scopus: 2-s2.0-0034675663
Elibrary: 13347861
Chemical Abstracts: 2000:755568
Chemical Abstracts (print): 134:71226
OpenAlex: W2069116279
Citing:
DB Citing
Web of science 17
Scopus 19
Elibrary 19
OpenAlex 22
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